Online advertising platforms use automated auctions to connect advertisers with potential customers, requiring effective bidding strategies to maximize profits. Accurate ad impact estimation requires considering three key factors: delayed and long-term effects, cumulative ad impacts such as reinforcement or fatigue, and customer heterogeneity. However, these effects are often not jointly addressed in previous studies. To capture these factors, we model ad bidding as a Contextual Markov Decision Process (CMDP) with delayed Poisson rewards. For efficient estimation, we propose a two-stage maximum likelihood estimator combined with data-splitting strategies, ensuring controlled estimation error based on the first-stage estimator's (in)accuracy. Building on this, we design a reinforcement learning algorithm to derive efficient personalized bidding strategies. This approach achieves a near-optimal regret bound of $\tilde{\mathcal{O}}(dH^2\sqrt{T})$, where $d$ is the contextual dimension, $H$ is the number of rounds, and $T$ is the number of customers. Our theoretical findings are validated by simulation experiments.

Understanding cellular responses to chemical interventions is critical to the discovery of effective therapeutics. Because individual biological techniques often measure only one axis of cellular response at a time, high-quality multimodal datasets are needed to unlock a holistic understanding of how cells respond to treatments and to advance computational methods that integrate modalities. However, many techniques destroy cells and thus preclude paired measurements, and attempts to match disparate unimodal datasets are often confounded by data being generated in incompatible experimental settings. Here we introduce scGeneScope, a multimodal single cell RNA sequencing (scRNA-seq) and Cell Painting microscopy image dataset conditionally paired by chemical treatment, designed to facilitate the development and benchmarking of unimodal, multimodal, and multiple profile machine learning methods for cellular profiling.

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Privacy and security concerns are becoming increasingly critical for recommender systems, as model extraction attack provides an effective way to probe system robustness by replicating the model's recommendation logic -- potentially exposing sensitive user preferences and proprietary algorithmic knowledge. Despite the promising performance of existing model extraction methods, they still face two key challenges: unrealistic assumptions on the requirement of accessible member or surrogate data and generalization problem where surrogate model architecture constraints lead to overfitting on generated data. To tackle these challenges, in this paper, we first thoroughly analyze how the architecture of surrogate models influences extraction attack performance, highlighting the superior effectiveness of the graph convolution architecture. Based on this, we propose a novel Data-free Black-box Graph convolution-based Recommender Model Extraction method, dubbed DBGRME. Specifically, DBGRME contains: (1) an interaction generator to alleviate the need for member data requirements in a data-free scenario; and (2) a generalization-aware graph convolution-based surrogate model to capture diverse and complex recommender interaction patterns for mitigating the overfitting issue. Experimental results on various datasets and victim models demonstrate the superiority of our attack in data-free scenarios (e.g., surpassing PTQ data-require methods with 17.4% improvement on LightGCN).

The design of biological sequences is essential for engineering functional biomolecules that contribute to advancements in human health and biotechnology. Recent advances in diffusion models, with their generative power and efficient conditional sampling, have made them a promising approach for sequence generation. To enhance model performance on limited data and enable multi-objective design and optimization, reinforcement learning (RL)-based fine-tuning has shown great potential. However, existing post-sampling and fine-tuning methods either lack stability in discrete optimization when avoiding gradients or incur high computational costs when employing gradient-based approaches, creating significant challenges for achieving both control and stability in the tuning process. To address these limitations, we propose GLID$^2$E, a gradient-free RL-based tuning approach for discrete diffusion models. Our method introduces a clipped likelihood constraint to regulate the exploration space and implements reward shaping to better align the generative process with design objectives, ensuring a more stable and efficient tuning process. By integrating these techniques, GLID$^2$E mitigates training instabilities commonly encountered in RL and diffusion-based frameworks, enabling robust optimization even in challenging biological design tasks. In the DNA sequence and protein sequence design systems, GLID$^2$E achieves competitive performance in function-based design while maintaining computational efficiency and a flexible tuning mechanism.

Traditional Chinese Medicine (TCM), as an effective alternative medicine, has been receiving increasing attention. In recent years, the rapid development of large language models (LLMs) tailored for TCM has highlighted the urgent need for an objective and comprehensive evaluation framework to assess their performance on real-world tasks. However, existing evaluation datasets are limited in scope and primarily text-based, lacking a unified and standardized multimodal question-answering (QA) benchmark. To address this issue, we introduce TCM-Ladder, the first comprehensive multimodal QA dataset specifically designed for evaluating large TCM language models. The dataset covers multiple core disciplines of TCM, including fundamental theory, diagnostics, herbal formulas, internal medicine, surgery, pharmacognosy, and pediatrics.

Autonomous AI agents that can follow instructions and perform complex multi-step tasks have tremendous potential to boost human productivity. However, to perform many of these tasks, the agents need access to personal information from their users, raising the question of whether they are capable of using it appropriately.

Invisible Image Watermarking is crucial for ensuring content provenance and accountability in generative AI. While Gen-AI providers are increasingly integrating invisible watermarking systems, the robustness of these schemes against forgery attacks remains poorly characterized. This is critical, as forging traceable watermarks onto illicit content leads to false attribution, potentially harming the reputation and legal standing of Gen-AI service providers who are not responsible for the content. In this work, we propose WMCopier, an effective watermark forgery attack that operates without requiring any prior knowledge of or access to the target watermarking algorithm.

Recent advances in generative models trained on large-scale datasets have enabled high-quality 3D synthesis across various domains. However, these models also raise critical privacy concerns. Unlike 2D image synthesis, where risks typically involve the leakage of visual features or identifiable patterns, 3D generation introduces additional challenges, as reconstructed shapes, textures, and spatial structures may inadvertently expose proprietary designs, biometric data, or other sensitive geometric information. This paper presents the first exploration of machine unlearning in 3D generation tasks. We investigate different unlearning objectives, including re-targeting and partial unlearning, and propose a novel framework that does not require full supervision of the unlearning target. To enable a more efficient unlearning process, we introduce a skip-acceleration mechanism, which leverages the similarity between multi-view generated images to bypass redundant computations. By establishing coherence across viewpoints during acceleration, our framework not only reduces computation but also enhances unlearning effectiveness, outperforming the non-accelerated baseline in both accuracy and efficiency. We conduct extensive experiments on the typical 3D generation models (Zero123 and Zero123XL), demonstrating that our approach achieves a 30\% speedup, while effectively unlearning target concepts without compromising generation quality. Our framework provides a scalable and practical solution for privacy-preserving 3D generation, ensuring responsible AI deployment in real-world applications.

DNA language models have revolutionized our ability to design and manipulate DNA sequences--the fundamental language of life--with unprecedented precision, enabling transformative applications in therapeutics, synthetic biology, and gene editing. However, this capability also poses significant dual-use risks, including the potential creation of harmful biological agents. To address these biosecurity challenges, we introduce two innovative watermarking techniques: DNAMark and CentralMark. DNAMark employs synonymous codon substitutions to embed robust watermarks in DNA sequences while preserving the function of encoded proteins. CentralMark advances this by creating inheritable watermarks that transfer from DNA to translated proteins, leveraging protein embeddings to ensure detection across the central dogma. Both methods utilize state-of-the-art embeddings to generate watermark logits, enhancing resilience against natural mutations, synthesis errors, and adversarial attacks. Evaluated on a therapeutic DNA benchmark, DNAMark and CentralMark achieve F1 detection scores above 0.85 under diverse conditions, while maintaining over 60\% sequence similarity to ground truth and degeneracy scores below 15\%. A case study on a CRISPR-Cas9 system underscores CentralMark's utility in real-world synthetic biology. This work establishes a vital framework for securing DNA language models, balancing innovation with accountability to mitigate biosecurity risks.